57000-78-9

Usage

Uses

Used in Agricultural and Horticultural Industries:
1-(4-Chlorophenoxy)-3,3-dimethyl-1-chloro-2-butanone is used as a selective herbicide for controlling broadleaf weeds in these industries. It is applied to target specific weed species, allowing for the protection and growth of desirable crops without causing harm to them.
Used in Pest Control:
In the context of pest control, 1-(4-Chlorophenoxy)-3,3-dimethyl-1-chloro-2-butanone serves as a pesticide, helping to manage and reduce the presence of unwanted plant species that can compete with cultivated crops for resources and potentially reduce yield.

InChI:InChI=1/C12H14Cl2O2/c1-12(2,3)10(15)11(14)16-9-6-4-8(13)5-7-9/h4-7,11H,1-3H3

Upstream product

• 24473-06-1 1-(4'-chlorophenoxy)-3,3-dimethyl-butan-2-one 
• 106-48-9 4-chloro-phenol 
• 75-97-8 3,3-dimethyl-butan-2-one 

Downstream Products

• 38083-17-9 climbazole 

Relevant academic research and scientific papers

NOVEL NEISSERIA MENINGITIDIS SEROGROUP Y OLIGOMER AND PROCESS FOR SYNTHESIZING THEREOF

The present invention relates to novel oligomers of Neisseria meningitidis serogroup Y capsular polysaccharide repeating unit (Men-Y oligomers) and process for synthesizing novel Men- Y oligomers. Inparticular, the present invention relates to the chemical synthesis of the tetramer of Men- Y capsular polysaccharide repeating unit capable of being used as a candidate in the development of semisynthetic or fully synthetic conjugate vaccine against meningococcal serogroup Y bacterial infection.

Preparation method of climbazole

The invention discloses a preparation method of climbazole. According to the method, toluene, chloroetherketone, imidazole and a catalyst, serving as raw materials, react under 100 DEG C to 110 DEG Cfor 4 hours while the temperature is kept, and then the climbazole with the purity being up to 99 percent is prepared by methods, such as crystallization, purification, alkaline wash and recrystallization. Through a lot of experiments, the invention screens out the best climbazole preparation method, the whole process design is reasonable, the process is easy and efficient to operate, in particular, the best reaction conditions screened out, which include catalyst variety, reaction solvent, reaction temperature, reaction time and steps, such as crude reaction of methylbenzene and the climbazole, and alkaline wash thereof, can greatly increase reaction yield (up to 92 percent or above), side reaction is reduced, the reaction rate is increased, the production cost is greatly reduced, and therefore the preparation method of the climbazole has a good application prospect.

Preparation of 3,3-dimethyl-1-phenoxy-butan-2-ols as fungicide intermediates

3,3-Dimethyl-1-phenoxy-butan-2-ols of the formula STR1 in which Y is a halogen atom, an optionally substituted phenyl radical, an optionally substituted phenoxy radical or a nitro, cyano, alkyl, alkoxy, alkoxycarbonyl or cycloalkyl radical, and n is 0, 1, 2 or 3, exhibit plant growth stimulating properties and are also useful in the synthesis of known fungicides. They are produced from tert-butyloxirane and the corresponding phenols.

Combating fungi with 1-azol-1-yl-1-phenoxy-2-alkane ethers

Azolyl ether derivatives of the formula STR1 in which A is CH or a nitrogen atom, R is alkyl, alkenyl, alkynyl, phenyl, benzyl or substituted phenyl or benzyl, X is halogen, alkyl, alkoxy, alkylthio, alkylsulphonyl, halogenoalkyl, alkoxycarbonyl, nitro, cyano, phenyl, phenoxy, phenylthio, or substituted phenyl, phenoxy of phenylthio, Y is alkyl, phenyl, or substituted alkyl or phenyl and n is 0, 1, 2, 3, 4 or 5, which possess fungicidal properties.

Antimicrobial agents and their use

The invention involves the provision of compositions containing a 3,3-dialkyl- or 3-aryl-phenoxy-1-(1,2,4-triazol-1-yl)- and (imidazol-1-yl-alkan-2-ol) ethers which are particularly effective as antimicrobial especially antimycotic, agents. The invention also includes use of said compositions for providing antimicrobial, particularly antimycotic effect.